EP2293765A2 - Composition après-shampoing possédant une limite d élasticité supérieure et un taux de conversion supérieur du composé gras en matrice gel - Google Patents

Composition après-shampoing possédant une limite d élasticité supérieure et un taux de conversion supérieur du composé gras en matrice gel

Info

Publication number
EP2293765A2
EP2293765A2 EP09770971A EP09770971A EP2293765A2 EP 2293765 A2 EP2293765 A2 EP 2293765A2 EP 09770971 A EP09770971 A EP 09770971A EP 09770971 A EP09770971 A EP 09770971A EP 2293765 A2 EP2293765 A2 EP 2293765A2
Authority
EP
European Patent Office
Prior art keywords
composition
melting point
hair
high melting
conditioning
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP09770971A
Other languages
German (de)
English (en)
Inventor
Jian-Zhong Yang
Toshiyuki Okada
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41445285&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP2293765(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to EP11193242.2A priority Critical patent/EP2460508B1/fr
Publication of EP2293765A2 publication Critical patent/EP2293765A2/fr
Ceased legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41—Amines
    • A61K8/416—Quaternary ammonium compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34—Alcohols
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34—Alcohols
    • A61K8/342—Alcohols having more than seven atoms in an unbroken chain
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42—Amides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/58—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • A61K8/585—Organosilicon compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • A61K8/731—Cellulose; Quaternized cellulose derivatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/12—Preparations containing hair conditioners
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/48—Thickener, Thickening system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/805—Corresponding aspects not provided for by any of codes A61K2800/81 - A61K2800/95

Definitions

  • WO 2006/044209 also describes that; preferably, the composition of the present invention comprises, by weight of the hair care composition, from about 60% to about 99% of a gel matrix including lamellar gel matrix.
  • the DSC profile shows a single peak having a peak top temperature of about 67°C to about 73°C, at about 8 mJ/mg, and no peaks larger than 2 mJ/mg from 40 0 C to about 65 0 C as the peaks showing at a temperature of from 40 0 C to 55 0 C mean the existence of high melting fatty compounds and/or cationic surfactants which are not incorporated into the gel matrix.
  • the present invention is directed to a hair conditioning composition
  • a hair conditioning composition comprising:
  • Fig. 1 illustrates an embodiment of d-spacing measurement of the lamellar gel matrix comprising lamella bilayers 1 and water 2.
  • composition (c) an aqueous carrier; wherein the cationic surfactant, the high melting point fatty compound, and the aqueous carrier form a gel matrix; wherein the composition has from about 90% to about 100% of a conversion rate of the high melting point fatty compound to the gel matrix; and wherein the composition has a yield point of about 33Pa or more.
  • cationic surfactants are those having a longer alkyl group, i.e., C18-22 alkyl group.
  • Such cationic surfactants include, for example, behenyl trimethyl ammonium chloride, methyl sulfate or ethyl sulfate, and stearyl trimethyl ammonium chloride, methyl sulfate or ethyl sulfate. Further preferred are behenyl trimethyl ammonium chloride, methyl sulfate or ethyl sulfate, and still further preferred is behenyl trimethyl ammonium chloride.
  • alkylamino substituted silicone compounds include those having alkylamino substitutions as pendant groups of a silicone backbone. Highly preferred are those known as "amodimethicone". Commercially available amodimethicones useful herein include, for example, BY16-872 available from Dow Corning.
  • composition of the present invention may include other additional components, which may be selected by the artisan according to the desired characteristics of the final product and which are suitable for rendering the composition more cosmetically or aesthetically acceptable or to provide them with additional usage benefits.
  • additional components generally are used individually at levels of from about 0.001% to about 10%, preferably up to about 5% by weight of the composition.
  • Low melting point oils useful herein are those having a melting point of less than 25°C.
  • the low melting point oil useful herein is selected from the group consisting of: hydrocarbon having from 10 to about 40 carbon atoms; unsaturated fatty alcohols having from about 10 to about 30 carbon atoms such as oleyl alcohol; unsaturated fatty acids having from about 10 to about 30 carbon atoms; fatty acid derivatives; fatty alcohol derivatives; ester oils such as pentaerythritol ester oils including pentaerythritol tetraisostearate, trimethylol ester oils, citrate ester oils, and glyceryl ester oils; poly ⁇ -olefin oils such as polydecenes; and mixtures thereof.
  • the method further comprises the step of adding additional ingredients such as silicone compounds, perfumes, preservatives, if included, to the gel matrix.
  • additional ingredients such as silicone compounds, perfumes, preservatives, if included
  • the premix and the aqueous carrier are mixed by using a high shear homogenizer.
  • a high shear homogenizer useful herein include, for example: Sonolator ® available from Sonic Corporation, Manton Gaulin type homogenizer available from the APV Manton Corporation, the Microfluidizer available from Microfluidics Corporation, Becomix ® available from A. Berents Gmbh&Co..
  • the total amount of the cationic surfactant and the high melting point fatty compound is from about 7.0%, preferably from about 7.5%, more preferably from about 8.0% by weight of the composition, in view of providing the benefits of the present invention, and to about 15%, preferably to about 14%, more preferably to about 13%, still more preferably to about 10% by weight of the composition, in view of spreadability and product appearance.
  • the method further requires at least one of the following: the mixing step (3) is conducted by using a homogenizer having a rotating member; the surfactant is a mono-alkyl cationic surfactant and the composition is substantially free of di-alkyl cationic surfactants; and the surfactant is a cationic surfactant and the oil phase contains from 0 to about 50% of the aqueous carrier by weight of the oil phase, preferably the oil phase is substantially free of water.
  • compositions of "Ex. 1" through “Ex. 4" and the composition of "Ex. iii” are suitably made as follows:
  • Cationic surfactants and high melting point fatty compounds are mixed and heated to from about 65°C to about 90 0 C to form a premix.
  • water is prepared at from about 25°C to about 52°C.
  • Becomix® direct injection rotor-stator homogenizer the premix is injected to a high shear field having an energy density of from 1.OxIO 4 J/m 3 to LOxIO 7 J/m 3 where the water is already present.
  • a gel matrix is formed. If included, silicone compounds, perfumes, preservatives are added to the gel matrix with agitation. Then the composition is cooled down to room temperature.
  • compositions of "Ex. i" and “Ex. ii” as shown above can be prepared by any conventional method well known in the art. They are suitably made as follows: If included, polymers are added to water with agitation. Cationic surfactants and high melting point fatty compounds are added to water with agitation, and heated to about 80 0 C. The mixture is cooled down to about 55°C and gel matrix is formed. If included, silicone compounds, perfumes, preservatives are added to the gel matrix with agitation. Then the mixture is cooled down to room temperature. Properties and Conditioning benefits
  • Dry conditioning performance is evaluated by hair friction force measured by an instrument named Instron Tester (Instron 5542, Instron, Inc,; Canton, Mass., USA). 2g of the composition is applied to 2Og of hair sample. After spreading the composition on the hair sample, rinsing it with warm water for 30 seconds, and the hair sample is left to dry over night. The friction force (g) between the hair surface and a urethane pad along the hair is measured.
  • the embodiments disclosed and represented by the previous "Ex. 1" through “Ex. 4" are hair conditioning compositions of the present invention which are particularly useful for rinse-off use.
  • Such embodiments have many advantages. For example, they provide improved conditioning benefits, especially improved wet conditioning benefits after rinsing and improved dry conditioning, while maintaining wet conditioning benefit before rinsing.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

La présente invention concerne une composition après-shampoing comprenant : (a) un tensioactif cationique; (b) un composé gras à point de fusion élevé; et (c) un véhicule aqueux; le tensioactif cationique, le composé gras à point de fusion élevé et le véhicule aqueux formant une matrice gel; la composition possédant un taux de conversion du composé gras à point de fusion élevé en matrice gel compris entre 90 % et 100 % environ; et la composition possédant une limite d’élasticité d’environ 33 Pa ou plus. La présente invention concerne également un procédé de fabrication de compositions après-shampoing. Les compositions de la présente invention et les compositions fabriquées en utilisant le procédé de la présente invention offrent des avantages de conditionnement améliorés, en particulier des avantages de conditionnement sur cheveux mouillés après rinçage améliorés et un conditionnement sur cheveux secs amélioré, tout en conservant l’avantage du conditionnement sur cheveux mouillés avant rinçage.
EP09770971A 2008-06-25 2009-06-25 Composition après-shampoing possédant une limite d élasticité supérieure et un taux de conversion supérieur du composé gras en matrice gel Ceased EP2293765A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP11193242.2A EP2460508B1 (fr) 2008-06-25 2009-06-25 Composition après-shampoing possédant une limite d élasticité supérieure et un taux de conversion supérieur du composé gras en matrice gel

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US13300208P 2008-06-25 2008-06-25
PCT/US2009/048533 WO2009158438A2 (fr) 2008-06-25 2009-06-25 Composition après-shampoing possédant une limite d’élasticité supérieure et un taux de conversion supérieur du composé gras en matrice gel

Related Child Applications (1)

Application Number Title Priority Date Filing Date
EP11193242.2A Division EP2460508B1 (fr) 2008-06-25 2009-06-25 Composition après-shampoing possédant une limite d élasticité supérieure et un taux de conversion supérieur du composé gras en matrice gel

Publications (1)

Publication Number Publication Date
EP2293765A2 true EP2293765A2 (fr) 2011-03-16

Family

ID=41445285

Family Applications (2)

Application Number Title Priority Date Filing Date
EP09770971A Ceased EP2293765A2 (fr) 2008-06-25 2009-06-25 Composition après-shampoing possédant une limite d élasticité supérieure et un taux de conversion supérieur du composé gras en matrice gel
EP11193242.2A Revoked EP2460508B1 (fr) 2008-06-25 2009-06-25 Composition après-shampoing possédant une limite d élasticité supérieure et un taux de conversion supérieur du composé gras en matrice gel

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP11193242.2A Revoked EP2460508B1 (fr) 2008-06-25 2009-06-25 Composition après-shampoing possédant une limite d élasticité supérieure et un taux de conversion supérieur du composé gras en matrice gel

Country Status (6)

Country Link
US (3) US20090324530A1 (fr)
EP (2) EP2293765A2 (fr)
JP (1) JP2011525540A (fr)
CN (2) CN102164578B (fr)
MX (1) MX2010013985A (fr)
WO (1) WO2009158438A2 (fr)

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WO2009158438A3 (fr) 2011-01-20
US20090324530A1 (en) 2009-12-31
CN102164578A (zh) 2011-08-24
US20120258067A1 (en) 2012-10-11
US8828370B2 (en) 2014-09-09
EP2460508A1 (fr) 2012-06-06
CN104083290B (zh) 2018-02-16
CN102164578B (zh) 2014-08-27
US20140356307A1 (en) 2014-12-04
JP2011525540A (ja) 2011-09-22
EP2460508B1 (fr) 2016-11-02
MX2010013985A (es) 2011-01-21
CN104083290A (zh) 2014-10-08
WO2009158438A2 (fr) 2009-12-30
US10413497B2 (en) 2019-09-17

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